Variant report

Variant	rs793496
Chromosome Location	chr3:99507254-99507255
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:99497311..99499461-chr3:99505852..99508651,2	K562	blood:
2	chr3:99506097..99508207-chr3:99511088..99512864,2	K562	blood:

Extended variants
information (count: 69 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1016914	0.83[CHB][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs1021102	0.83[CHB][hapmap];0.90[JPT][hapmap];0.88[YRI][hapmap]
rs1021103	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1038294	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1087198	0.83[CHB][hapmap];0.82[CHD][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap]
rs10936005	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10936008	0.91[JPT][hapmap]
rs1287283	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs13317017	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs16841679	0.81[CHB][hapmap]
rs1688766	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1688771	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1688772	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1688782	0.83[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap]
rs1718246	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2452320	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs2452321	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs4075038	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.93[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4244711	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs4244713	0.90[JPT][hapmap];0.89[YRI][hapmap]
rs4361315	0.86[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.93[MEX][hapmap];0.96[TSI][hapmap];0.80[YRI][hapmap]
rs4479633	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs4571265	0.86[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.90[MKK][hapmap];0.96[TSI][hapmap];0.89[YRI][hapmap]
rs4928149	1.00[ASW][hapmap];0.93[CEU][hapmap];0.80[GIH][hapmap]
rs4928232	0.91[JPT][hapmap];0.89[YRI][hapmap]
rs629120	0.84[ASW][hapmap];1.00[YRI][hapmap]
rs6440938	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs6765027	0.91[JPT][hapmap];0.89[YRI][hapmap]
rs6809988	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs694429	0.84[ASW][hapmap];1.00[YRI][hapmap]
rs704570	0.81[JPT][hapmap];0.80[YRI][hapmap]
rs704573	0.81[JPT][hapmap]
rs704581	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs704582	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];0.95[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs704583	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs7616988	0.94[CEU][hapmap];0.94[GIH][hapmap];0.90[JPT][hapmap];0.80[MEX][hapmap];0.89[TSI][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7629426	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs7636447	0.83[CHB][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs7638900	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs792834	0.93[CEU][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs793440	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs793445	0.83[CHB][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs793452	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs793453	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs793457	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs793460	0.83[CHB][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs793461	0.83[CHB][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs793462	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs793463	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs793465	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs793466	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs793467	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap]
rs793468	0.83[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap]
rs793470	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs793472	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs793474	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs793488	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs793492	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs793494	0.83[CHB][hapmap];0.83[CHD][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap]
rs793495	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap]
rs793499	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.86[MEX][hapmap];0.95[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs793503	0.83[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap]
rs796977	0.83[CHB][hapmap];0.90[JPT][hapmap];0.80[YRI][hapmap]
rs796978	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs809415	0.83[CHB][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs812657	0.83[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]
rs9872871	0.83[CHB][hapmap];0.91[JPT][hapmap];0.89[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817478	chr3:99474086-99955548	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv916476	chr3:99478229-100124625	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs793496	FILIP1L	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99492000-99517600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr3:99494200-99513600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:99496000-99513000	Weak transcription	NHEK	skin
4	chr3:99499400-99509000	Weak transcription	Aorta	Aorta
5	chr3:99501000-99513000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:99501400-99509000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:99502400-99508800	Weak transcription	Adipose Nuclei	Adipose
8	chr3:99502600-99518200	Weak transcription	HSMMtube	muscle
9	chr3:99502800-99508200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:99502800-99518400	Weak transcription	NH-A	brain
11	chr3:99503600-99509000	Weak transcription	HUVEC	blood vessel
12	chr3:99504600-99513000	Weak transcription	HSMM	muscle
13	chr3:99505400-99507600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr3:99505800-99513200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:99506200-99507400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr3:99506400-99508200	Weak transcription	Fetal Lung	lung
17	chr3:99506600-99507600	Enhancers	Rectal Smooth Muscle	rectum
18	chr3:99506800-99507600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr3:99507200-99507400	Enhancers	NHLF	lung
20	chr3:99507200-99507800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:99507200-99508200	Enhancers	Osteobl	bone
22	chr3:99507200-99508400	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links