Variant report

Variant	rs28535536
Chromosome Location	chr9:98226702-98226703
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:98222216..98224760-chr9:98225950..98227870,2	MCF-7	breast:
2	chr9:98223864..98226761-chr9:98228381..98231062,3	K562	blood:
3	chr9:98223555..98229775-chr9:98269693..98275962,10	K562	blood:
4	chr9:98218910..98222494-chr9:98224731..98227835,5	K562	blood:
5	chr9:98222977..98229750-chr9:98267050..98274823,12	K562	blood:
6	chr9:98223412..98227347-chr9:98253313..98257210,3	K562	blood:

Variant related genes	Relation type
ENSG00000271314	Chromatin interaction
ENSG00000185920	Chromatin interaction
ENSG00000271155	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10512249	0.87[ASW][hapmap];0.91[CEU][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.81[YRI][hapmap];0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs16909892	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16909898	1.00[ASW][hapmap];0.91[CEU][hapmap];0.88[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.91[TSI][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16909902	0.91[CEU][hapmap];0.88[JPT][hapmap];0.90[TSI][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16909904	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16909922	0.83[EUR][1000 genomes]
rs1805155	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2036963	0.87[EUR][1000 genomes]
rs2282040	0.87[ASW][hapmap];0.91[CEU][hapmap];0.88[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs2282041	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2282043	0.83[CEU][hapmap];0.87[EUR][1000 genomes]
rs28372566	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28418339	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28427480	0.83[EUR][1000 genomes]
rs28446116	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28446321	0.83[EUR][1000 genomes]
rs28448271	0.83[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs28469297	1.00[MEX][hapmap]
rs28474857	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs28493225	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28494679	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28510415	0.88[EUR][1000 genomes]
rs28520225	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28535421	0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28583690	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28601668	0.84[LWK][hapmap]
rs28673156	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs28706464	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28711421	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28733891	0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3780573	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3824488	0.83[CEU][hapmap];0.85[JPT][hapmap];0.88[EUR][1000 genomes]
rs56149656	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59015093	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59925771	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60150206	0.82[EUR][1000 genomes]
rs60417486	0.82[EUR][1000 genomes]
rs867452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531633	chr9:98078300-98431120	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv831658	chr9:98152971-98342178	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv949520	chr9:98204199-98238358	Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv430083	chr9:98204245-98445645	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1053762	chr9:98208542-98232120	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv1047465	chr9:98217524-98228225	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs28535536	PTCH1	Cis_1M	lymphoblastoid	RTeQTL
rs28535536	FBP2	cis	parietal	SCAN

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98206000-98237600	Weak transcription	Psoas Muscle	Psoas
2	chr9:98218800-98227400	Genic enhancers	Fetal Stomach	stomach
3	chr9:98221800-98232400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr9:98223400-98266400	Weak transcription	Hela-S3	cervix
5	chr9:98223600-98227600	Weak transcription	A549	lung
6	chr9:98224000-98228800	Weak transcription	Liver	Liver
7	chr9:98224200-98227200	Weak transcription	Gastric	stomach
8	chr9:98224200-98227600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:98224200-98228000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr9:98224200-98228800	Weak transcription	Right Ventricle	heart
11	chr9:98224200-98229000	Weak transcription	Esophagus	oesophagus
12	chr9:98224400-98228800	Weak transcription	HepG2	liver
13	chr9:98224600-98228800	Weak transcription	Aorta	Aorta
14	chr9:98225000-98226800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:98225000-98227200	Weak transcription	Small Intestine	intestine
16	chr9:98225000-98228200	Genic enhancers	Fetal Lung	lung
17	chr9:98225000-98228800	Weak transcription	Lung	lung
18	chr9:98225200-98229000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr9:98225600-98226800	Enhancers	Muscle Satellite Cultured Cells	--
20	chr9:98225600-98227000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:98225600-98227000	Enhancers	Brain Angular Gyrus	brain
22	chr9:98225600-98227200	Weak transcription	Ovary	ovary
23	chr9:98225600-98229200	Weak transcription	Spleen	Spleen
24	chr9:98225600-98234000	Weak transcription	Right Atrium	heart
25	chr9:98225800-98226800	Enhancers	Fetal Thymus	thymus
26	chr9:98225800-98227000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr9:98225800-98227200	Enhancers	Brain Cingulate Gyrus	brain
28	chr9:98225800-98227400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:98225800-98227400	Weak transcription	Adipose Nuclei	Adipose
30	chr9:98225800-98227400	Enhancers	Brain Hippocampus Middle	brain
31	chr9:98225800-98227400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr9:98225800-98228800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:98225800-98228800	Enhancers	Brain Germinal Matrix	brain
34	chr9:98225800-98229000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr9:98225800-98229000	Weak transcription	Colon Smooth Muscle	Colon
36	chr9:98225800-98239600	Weak transcription	HMEC	breast
37	chr9:98225800-98239800	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr9:98225800-98244000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr9:98226000-98226800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr9:98226000-98226800	Genic enhancers	Duodenum Mucosa	Duodenum
41	chr9:98226000-98227200	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr9:98226000-98227800	Genic enhancers	K562	blood
43	chr9:98226000-98228000	Weak transcription	Left Ventricle	heart
44	chr9:98226000-98228400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr9:98226000-98229000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr9:98226000-98229000	Weak transcription	Rectal Smooth Muscle	rectum
47	chr9:98226000-98229200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr9:98226000-98229400	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr9:98226000-98248400	Weak transcription	HUVEC	blood vessel
50	chr9:98226000-98251000	Weak transcription	Osteobl	bone

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links