Variant report

Variant	rs72785845
Chromosome Location	chr5:106767672-106767673
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs3909463	1.00[AFR][1000 genomes]
rs62357486	1.00[AFR][1000 genomes]

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	nsv1030118	chr5:106006097-106847949	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106751800-106767800	Weak transcription	Stomach Mucosa	stomach
2	chr5:106756400-106768200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr5:106756600-106772000	Weak transcription	Esophagus	oesophagus
4	chr5:106758600-106767800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:106758600-106767800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr5:106758600-106767800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr5:106758600-106767800	Weak transcription	Left Ventricle	heart
8	chr5:106758600-106771200	Weak transcription	Right Ventricle	heart
9	chr5:106758600-106772000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:106758600-106785000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr5:106762200-106771600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr5:106762200-106772200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:106763000-106772000	Weak transcription	Right Atrium	heart
14	chr5:106763200-106767800	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr5:106763200-106773600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:106763200-106773600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:106763400-106771800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:106766200-106772000	Weak transcription	Brain Germinal Matrix	brain
19	chr5:106766400-106767800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:106766400-106767800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr5:106766400-106771200	Weak transcription	Fetal Kidney	kidney
22	chr5:106766400-106775200	Weak transcription	Aorta	Aorta
23	chr5:106766600-106770400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr5:106767000-106768600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr5:106767000-106768600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr5:106767200-106768000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr5:106767200-106768400	Enhancers	Hela-S3	cervix
28	chr5:106767200-106768600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:106767200-106768600	Enhancers	HMEC	breast
30	chr5:106767400-106767800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:106767400-106767800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:106767400-106767800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:106767400-106767800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr5:106767400-106767800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:106767400-106767800	Flanking Active TSS	NHDF-Ad	bronchial
36	chr5:106767400-106768000	Enhancers	Brain Angular Gyrus	brain
37	chr5:106767400-106768000	Flanking Active TSS	A549	lung
38	chr5:106767400-106768200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr5:106767400-106768400	Enhancers	Osteobl	bone
40	chr5:106767400-106768600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr5:106767400-106768600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:106767400-106768600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr5:106767400-106768600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr5:106767400-106768600	Enhancers	HSMM	muscle
45	chr5:106767400-106768600	Enhancers	HUVEC	blood vessel
46	chr5:106767400-106768600	Enhancers	NHEK	skin
47	chr5:106767400-106768600	Enhancers	NHLF	lung
48	chr5:106767600-106767800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:106767600-106767800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:106767600-106767800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links