Variant report

Variant	rs28403152
Chromosome Location	chr9:16670162-16670163
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10962529	0.88[AFR][1000 genomes]
rs12343524	0.82[AFR][1000 genomes]
rs28575837	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1032856	chr9:16465330-16773471	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv540073	chr9:16465330-16773471	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv430000	chr9:16603483-16671045	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	esv2758627	chr9:16641966-16809203	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	esv2759673	chr9:16641966-16809203	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv892648	chr9:16661092-16680901	Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16640000-16670800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:16656600-16670800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:16657600-16670800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:16657600-16670800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:16657600-16671000	Weak transcription	NH-A	brain
6	chr9:16657600-16681400	Weak transcription	Psoas Muscle	Psoas
7	chr9:16659800-16670800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr9:16662400-16671000	Weak transcription	HSMM	muscle
9	chr9:16663400-16671000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr9:16664400-16671400	Weak transcription	A549	lung
11	chr9:16665000-16704400	Weak transcription	Aorta	Aorta
12	chr9:16667000-16670400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr9:16667200-16671800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr9:16667200-16681000	Weak transcription	Fetal Stomach	stomach
15	chr9:16667400-16671200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr9:16667600-16671400	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:16668400-16672200	Enhancers	Osteobl	bone
18	chr9:16668400-16679000	Weak transcription	Ovary	ovary
19	chr9:16668600-16672000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:16668800-16679600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr9:16669000-16681400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr9:16669200-16671000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr9:16669400-16672200	Enhancers	Fetal Kidney	kidney
24	chr9:16669800-16670200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:16669800-16670200	Weak transcription	NHDF-Ad	bronchial
26	chr9:16669800-16670800	Weak transcription	NHLF	lung
27	chr9:16670000-16670800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links