Variant report

Variant	rs143234805
Chromosome Location	chr17:15689204-15689205
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916652	chr17:15093600-15856310	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1059056	chr17:15294011-15856861	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
4	nsv1062951	chr17:15561070-15890644	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv1066023	chr17:15607267-16053512	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv907705	chr17:15611495-15717546	ZNF genes & repeats Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
8	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
9	nsv1061222	chr17:15672934-15999778	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
10	nsv442411	chr17:15677001-15694785	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island	6 gene(s)	inside rSNPs	diseases
11	esv3406800	chr17:15688452-15691000	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
12	esv3342426	chr17:15688677-15690975	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15686400-15689400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr17:15686400-15689400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr17:15686600-15689400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr17:15686600-15689400	Weak transcription	Aorta	Aorta
5	chr17:15686600-15689400	Weak transcription	Colonic Mucosa	Colon
6	chr17:15686600-15689400	Weak transcription	Fetal Muscle Leg	muscle
7	chr17:15686600-15689400	Weak transcription	Left Ventricle	heart
8	chr17:15686600-15689400	Weak transcription	HMEC	breast
9	chr17:15686600-15689600	Weak transcription	Brain Germinal Matrix	brain
10	chr17:15686600-15689600	Weak transcription	Esophagus	oesophagus
11	chr17:15686600-15689600	Weak transcription	Lung	lung
12	chr17:15686600-15689600	Weak transcription	Pancreas	Pancrea
13	chr17:15686600-15689600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr17:15686600-15689600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr17:15686600-15689600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr17:15686600-15689800	Weak transcription	Placenta	Placenta
17	chr17:15686600-15690600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr17:15686600-15691400	Weak transcription	Gastric	stomach
19	chr17:15686800-15689400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr17:15687000-15689400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr17:15687800-15689400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr17:15687800-15689400	Weak transcription	Psoas Muscle	Psoas
23	chr17:15687800-15689600	Weak transcription	Colon Smooth Muscle	Colon
24	chr17:15687800-15690000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr17:15688200-15689400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr17:15688200-15689600	Weak transcription	Fetal Lung	lung
27	chr17:15689000-15689400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr17:15689000-15689400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr17:15689000-15690000	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr17:15689000-15690200	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr17:15689000-15690200	Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr17:15689000-15690200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr17:15689200-15689400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr17:15689200-15689400	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr17:15689200-15689400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr17:15689200-15689400	Enhancers	Fetal Heart	heart
37	chr17:15689200-15689400	Weak transcription	Fetal Stomach	stomach
38	chr17:15689200-15689400	Enhancers	A549	lung
39	chr17:15689200-15689400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr17:15689200-15689400	Flanking Active TSS	NHLF	lung
41	chr17:15689200-15689800	Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr17:15689200-15690000	Active TSS	Muscle Satellite Cultured Cells	--
43	chr17:15689200-15690000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr17:15689200-15690000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr17:15689200-15690000	Active TSS	Right Atrium	heart
46	chr17:15689200-15690000	Active TSS	HUVEC	blood vessel
47	chr17:15689200-15690000	Active TSS	NHDF-Ad	bronchial
48	chr17:15689200-15690200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr17:15689200-15690200	Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr17:15689200-15690200	Active TSS	HUES64 Cell Line	embryonic stem cell

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