Variant report

Variant	rs17450667
Chromosome Location	chr8:118871391-118871392
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10090920	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10091596	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10094440	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10094527	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10098149	1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10098896	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.91[AFR][1000 genomes]
rs10098992	0.89[CHB][hapmap];0.90[JPT][hapmap]
rs10102974	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs10103242	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10103734	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10105753	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10107623	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10109017	1.00[JPT][hapmap]
rs10109062	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10111197	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10111573	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10111990	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10113092	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12675718	0.82[JPT][hapmap]
rs17430042	0.81[JPT][hapmap]
rs17430154	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17430175	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17430182	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17430252	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17430273	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17430294	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17430301	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17439791	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17439798	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17439812	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17439840	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17439847	0.89[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs17439868	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17450494	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs17450612	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17450661	0.85[CHB][hapmap];0.81[JPT][hapmap];0.87[YRI][hapmap];0.91[AFR][1000 genomes]
rs17450681	1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17452687	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17474672	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17474679	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17474839	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17503377	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17503447	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2067866	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs6987177	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7835395	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9656922	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs9792392	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019636	chr8:118598433-118946091	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv539734	chr8:118598433-118946091	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv831439	chr8:118747352-118899118	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv933516	chr8:118764605-119009093	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1030459	chr8:118840179-119155835	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118860800-118874800	Weak transcription	Lung	lung
2	chr8:118861000-118874200	Weak transcription	A549	lung
3	chr8:118861200-118875000	Weak transcription	Right Ventricle	heart
4	chr8:118861400-118872400	Weak transcription	Aorta	Aorta
5	chr8:118861400-118878600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:118861600-118876200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:118861600-118878200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:118863200-118872600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:118863200-118874400	Weak transcription	Stomach Mucosa	stomach
10	chr8:118863200-118879600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr8:118863400-118873000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr8:118863400-118874200	Weak transcription	HSMM	muscle
13	chr8:118863400-118874600	Weak transcription	HUVEC	blood vessel
14	chr8:118863400-118874800	Weak transcription	NH-A	brain
15	chr8:118863600-118872600	Weak transcription	NHLF	lung
16	chr8:118864000-118872400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr8:118864200-118872600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:118864200-118874800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:118864200-118878600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr8:118864600-118873000	Weak transcription	Osteobl	bone
21	chr8:118866600-118872600	Weak transcription	Small Intestine	intestine
22	chr8:118866600-118874600	Weak transcription	Duodenum Mucosa	Duodenum
23	chr8:118867000-118872600	Weak transcription	NHDF-Ad	bronchial
24	chr8:118869800-118872600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr8:118870000-118874400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:118870000-118876000	Weak transcription	Fetal Intestine Small	intestine
27	chr8:118870000-118876600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr8:118870200-118871400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr8:118870200-118872600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:118870400-118871400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr8:118870400-118871600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr8:118870600-118874200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links