Variant report

Variant	rs114922139
Chromosome Location	chr8:119628671-119628672
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv891413	chr8:119607281-119679668	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv1814789	chr8:119627671-119672134	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv465786	chr8:119627671-119767165	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv612048	chr8:119627671-119767165	Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119605800-119631800	Weak transcription	Fetal Intestine Small	intestine
2	chr8:119609200-119633000	Weak transcription	Gastric	stomach
3	chr8:119609400-119633600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:119619400-119632200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:119623200-119632200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr8:119623800-119632800	Weak transcription	Fetal Lung	lung
7	chr8:119624200-119632800	Weak transcription	Pancreas	Pancrea
8	chr8:119625200-119632000	Weak transcription	Fetal Intestine Large	intestine
9	chr8:119626400-119630600	Enhancers	Brain Angular Gyrus	brain
10	chr8:119626600-119629000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:119626600-119629000	Enhancers	Brain Anterior Caudate	brain
12	chr8:119626600-119630600	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr8:119626800-119630800	Enhancers	Brain Hippocampus Middle	brain
14	chr8:119627000-119628800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr8:119627000-119632000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr8:119627000-119632200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr8:119627000-119632400	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr8:119627200-119633200	Weak transcription	Aorta	Aorta
19	chr8:119627600-119629200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr8:119627600-119630600	Enhancers	Brain Substantia Nigra	brain
21	chr8:119627600-119632800	Weak transcription	NHEK	skin
22	chr8:119627600-119633600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:119627800-119630000	Enhancers	Brain Cingulate Gyrus	brain
24	chr8:119627800-119632000	Weak transcription	GM12878-XiMat	blood
25	chr8:119627800-119632400	Weak transcription	Left Ventricle	heart
26	chr8:119627800-119632400	Weak transcription	Right Atrium	heart
27	chr8:119627800-119632800	Weak transcription	Colonic Mucosa	Colon
28	chr8:119627800-119632800	Weak transcription	Spleen	Spleen
29	chr8:119628000-119631200	Weak transcription	Lung	lung
30	chr8:119628000-119632800	Weak transcription	Esophagus	oesophagus
31	chr8:119628000-119633000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr8:119628200-119628800	Enhancers	NH-A	brain
33	chr8:119628600-119628800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr8:119628600-119628800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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