Variant report

Variant	rs7758317
Chromosome Location	chr6:45536610-45536611
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1041334	0.88[ASN][1000 genomes]
rs10807322	0.84[ASN][1000 genomes]
rs12192817	0.81[ASN][1000 genomes]
rs12202314	0.85[ASN][1000 genomes]
rs12204264	0.83[ASN][1000 genomes]
rs12664797	0.95[ASN][1000 genomes]
rs16873510	0.88[ASN][1000 genomes]
rs1928529	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1928530	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1928531	0.86[ASN][1000 genomes]
rs1928532	0.91[ASN][1000 genomes]
rs3763191	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6913882	0.83[ASN][1000 genomes]
rs6914235	0.83[ASN][1000 genomes]
rs6938450	0.83[CHB][hapmap]
rs7752324	0.97[ASN][1000 genomes]
rs7758107	0.97[ASN][1000 genomes]
rs9463100	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv427755	chr6:45474631-45627025	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv532024	chr6:45475088-45982640	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS 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	21 gene(s)	inside rSNPs	diseases
5	nsv603009	chr6:45530471-45543530	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv462940	chr6:45532214-45545975	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv603010	chr6:45532214-45545975	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45522000-45536800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr6:45524800-45537000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:45531000-45537000	Weak transcription	Ovary	ovary
4	chr6:45531000-45537200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:45532400-45537000	Weak transcription	Fetal Heart	heart
6	chr6:45533800-45537400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:45534000-45537600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr6:45534200-45537800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:45534200-45538000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:45534400-45537600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:45534400-45538000	Enhancers	HMEC	breast
12	chr6:45534600-45537800	Enhancers	NHEK	skin
13	chr6:45535000-45537000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr6:45535000-45537000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:45535000-45537200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:45535200-45537000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr6:45535200-45537000	Weak transcription	HSMM	muscle
18	chr6:45535400-45536800	Weak transcription	HSMMtube	muscle
19	chr6:45535400-45537200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr6:45535400-45537200	Weak transcription	NH-A	brain
21	chr6:45535400-45539000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr6:45536000-45536800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:45536000-45538000	Enhancers	Dnd41	blood
24	chr6:45536200-45537600	Enhancers	Left Ventricle	heart
25	chr6:45536200-45537600	Enhancers	Right Atrium	heart
26	chr6:45536400-45537400	Enhancers	Esophagus	oesophagus
27	chr6:45536600-45537200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr6:45536600-45537200	Enhancers	Fetal Thymus	thymus
29	chr6:45536600-45537600	Enhancers	Lung	lung
30	chr6:45536600-45537800	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links